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通过计算机生物信息学分析,随后使用存档的福尔马林固定石蜡包埋(FFPE)组织活检进行分子验证,确定了一组与重度哮喘和肺癌相关的转录本。

In Silico Bioinformatics Followed by Molecular Validation Using Archival FFPE Tissue Biopsies Identifies a Panel of Transcripts Associated with Severe Asthma and Lung Cancer.

作者信息

Salameh Laila, Bhamidimarri Poorna Manasa, Saheb Sharif-Askari Narjes, Dairi Youssef, Hammoudeh Sarah Musa, Mahdami Amena, Alsharhan Mouza, Tirmazy Syed Hammad, Rawat Surendra Singh, Busch Hauke, Hamid Qutayba, Al Heialy Saba, Hamoudi Rifat, Mahboub Bassam

机构信息

Sharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah 27272, United Arab Emirates.

Dubai Health Authority, Dubai 4545, United Arab Emirates.

出版信息

Cancers (Basel). 2022 Mar 25;14(7):1663. doi: 10.3390/cancers14071663.

Abstract

Severe asthma and lung cancer are both heterogeneous pathological diseases affecting the lung tissue. Whilst there are a few studies that suggest an association between asthma and lung cancer, to the best of our knowledge, this is the first study to identify common genes involved in both severe asthma and lung cancer. Publicly available transcriptomic data for 23 epithelial brushings from severe asthmatics and 55 samples of formalin-fixed paraffin-embedded (FFPE) lung cancer tissue at relatively early stages were analyzed by absolute gene set enrichment analysis (GSEA) in comparison to 37 healthy bronchial tissue samples. The key pathways enriched in asthmatic patients included adhesion, extracellular matrix, and epithelial cell proliferation, which contribute to tissue remodeling. In the lung cancer dataset, the main pathways identified were receptor tyrosine kinase signaling, wound healing, and growth factor response, representing the early cancer pathways. Analysis of the enriched genes derived from the pathway analysis identified seven genes expressed in both the asthma and lung cancer sets: , , , , , , and . The differential expression of these genes was validated in vitro in the cell lines retrieved from different lung cancer and severe asthma patients using real-time PCR. The effect of the expression of the seven genes identified in the study on the overall survival of lung cancer patients ( = 1925) was assessed using a Kaplan-Meier plot. In vivo validation performed in the archival biopsies obtained from patients diagnosed with both the disease conditions provided interesting insights into the pathogenesis of severe asthma and lung cancer, as indicated by the differential expression pattern of the seven transcripts in the mixed group as compared to the asthmatics and lung cancer samples alone.

摘要

重度哮喘和肺癌都是影响肺组织的异质性病理疾病。虽然有一些研究表明哮喘与肺癌之间存在关联,但据我们所知,这是第一项确定重度哮喘和肺癌共同涉及基因的研究。通过绝对基因集富集分析(GSEA),对来自重度哮喘患者的23份上皮刷检样本以及相对早期的55份福尔马林固定石蜡包埋(FFPE)肺癌组织样本的公开转录组数据进行了分析,并与37份健康支气管组织样本进行了比较。哮喘患者中富集的关键通路包括黏附、细胞外基质和上皮细胞增殖,这些通路有助于组织重塑。在肺癌数据集中,确定的主要通路是受体酪氨酸激酶信号传导、伤口愈合和生长因子反应,代表了早期癌症通路。对通路分析得出的富集基因进行分析,确定了在哮喘和肺癌组中均表达的7个基因: 、 、 、 、 、 和 。使用实时PCR在从不同肺癌和重度哮喘患者中获取的细胞系中对这些基因的差异表达进行了体外验证。使用Kaplan-Meier图评估了该研究中确定的7个基因的表达对肺癌患者总体生存( = 1925)的影响。在从同时患有这两种疾病的患者获得的存档活检组织中进行的体内验证,揭示了重度哮喘和肺癌发病机制的有趣见解,这体现在混合组中7种转录本的差异表达模式与单独的哮喘患者和肺癌样本相比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e736/8996975/825ab8585e36/cancers-14-01663-g001.jpg

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